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- W2938241423 endingPage "49" @default.
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- W2938241423 abstract "This is an updated review of the literature on the emerging therapeutic options for the treatment of pemphigus to provide better care for patients. There is an increasing range of molecules targeted for pemphigus therapy against CD20, Bruton tyrosine kinase, chimeric antigen receptor, T-cell immune components, B-cell activating factor, proliferation-inducing ligand (APRIL), CD25, p38 mitogen-activated protein kinase (p38MAPK) and cytokine modulation therapies (anti-IL-4, anti-IL-6). The main aim of the current new therapies is to provide specific pathology-focused therapeutic options which have long-term sustainable therapeutic effects on disease progress, cause less side effects without systemic immunosuppression, and have less risk of getting antibodies against the medication during treatment." @default.
- W2938241423 created "2019-04-25" @default.
- W2938241423 creator A5000758369 @default.
- W2938241423 creator A5062955265 @default.
- W2938241423 date "2019-06-01" @default.
- W2938241423 modified "2023-09-27" @default.
- W2938241423 title "Pharmacological advances in pemphigus" @default.
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- W2938241423 doi "https://doi.org/10.1016/j.coph.2019.01.001" @default.
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